The following data is part of a premarket notification filed by Renal Systems, Inc. with the FDA for Concentrate Conductivity Meter.
| Device ID | K841543 |
| 510k Number | K841543 |
| Device Name: | CONCENTRATE CONDUCTIVITY METER |
| Classification | System, Dialysate Delivery, Central Multiple Patient |
| Applicant | RENAL SYSTEMS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FKQ |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-04-16 |
| Decision Date | 1984-05-22 |